| Literature DB >> 32180153 |
Hiroki Ishii1, Chiaki Miyoshi1, Keiji Hirai2, Junki Morino1, Saori Minato1, Shohei Kaneko1, Katsunori Yanai1, Momoko Matsuyama1, Taisuke Kitano1, Mitsutoshi Shindo1, Akinori Aomatsu1, Hiroshi Shimoyama1, Haruhisa Miyazawa1, Kiyonori Ito1, Yuichiro Ueda1, Yoshio Kaku1, Taro Hoshino1, Susumu Ookawara1, Yoshiyuki Morishita1.
Abstract
An 88-year-old man with congenital hemophilia A developed end-stage renal disease due to microscopic polyangiitis. He was at risk for catheter-related infection because he was taking immunosuppressive agents for the treatment of polyangiitis. He was also unable to manipulate the peritoneal dialysis device. Therefore, hemodialysis using an arteriovenous fistula was induced for renal replacement therapy. Recombinant coagulation factor VIII (1000 IU) was administered via the venous chamber of the hemodialysis circuit 10 min before the end of each hemodialysis session, and nafamostat mesylate (25 mg/h) was employed as an anticoagulant during hemodialysis. His clotting factor VIII activity level increased to > 50% and activated partial thromboplastin time decreased to 50 s at the end of each hemodialysis session. This method allowed him to achieve hemostasis at the puncture site of the arteriovenous fistula and undergo stable hemodialysis with no complications, including bleeding. This case suggests that hemodialysis using an arteriovenous fistula with coagulation factor replacement and nafamostat mesylate in each hemodialysis session is a therapeutic option for end-stage renal disease in patients of advanced age with hemophilia at high risk of bleeding.Entities:
Keywords: Arteriovenous fistula; Hemodialysis; Hemophilia; Microscopic polyangiitis; Nafamostat; Recombinant coagulation factor VIII
Year: 2020 PMID: 32180153 PMCID: PMC7320112 DOI: 10.1007/s13730-020-00461-1
Source DB: PubMed Journal: CEN Case Rep ISSN: 2192-4449